Impact Factor
3.88
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
3.81
2,388 total citations
h5-index
40
h5 depth signal
Cited share
83.0%
534 of 643
Total citations
2,388
Citation footprint
Metric signal
3.42
External metric anchor
Self-citation
5.9%
140 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
1,215
United States
822
Japan
348
Germany
269
South Korea
236
Citing Fields of Research
Phytochemicals
2,107
Mycotoxins
1,556
Synthesis
537
Bacteriology
410
Industrial Microbiology
389
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
17,106
Articles tracked across the journal lifetime
Indexed publication set
643
534 cited publications
Last 12 months
347
28.9 publications/month
Open access share
24.5%
85 OA publications in the last year
Leading citing country
China
1,215 citing publications
Leading citing field
Phytochemicals
2,107 citing publications
Latest tracked publication
20 October 2026
10 recent records available
Coverage & Indexing History
v42,Jan./Feb. 1979-
v42,Jan./Feb. 1979-
Active Coverage
Research Focus & Classification
Indexed Subjects
Mycotoxins
Phytochemicals
Synthesis
Bacteriology
Issuing & Sponsoring Bodies
Contributor
Lloyd Library and Museum
Contributor
American Society of Pharmacognosy
Broad Categories
Pharmacology
Mycotoxins
MeSH Descriptors
Pharmacognosy
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1021/acs.jnatprod.6c00649
Open DOI
Acid-Induced Wagner−Meerwein Rearrangements of Lupeol, Betulin, and Betulinic Acid and Synthesis of Allobetulin-Type Triterpenoids
Acid-induced skeletal rearrangements represent an inherent reactivity of lupane-type pentacyclic triterpenoids. This work provides a comprehensive review of these transformations, occurring through sequential Wagner−Meerwein-type 1,2-sup...
02
DOI 10.1021/acs.jnatprod.6c00880
Open DOI
Cytochalasin H Derivatives from the Marine-Derived Fungus Diaporthe sp. CS−HF−1 and Their Anti-Ferroptotic Activity in Human Proximal Tubular Epithelial Cells
Ferroptosis is a major driver of tubular necrosis, and its pharmacological inhibition markedly attenuates renal injury. In this study, chemical investigation of the marine-derived fungus Diaporthe sp. CS−HF−1 led to the identification of...
03
DOI 10.1021/acs.jnatprod.6c00845
Open DOI
Lavasamycins, Glycosylated Dihydroxyanthraquinones from Streptomyces barkulensis subsp. lavasanensis Subsp. nov.
Streptomyces sp. DSM 115979T, isolated from soil collected in Lavasan (Iran), was classified as a novel subspecies of Streptomyces barkulensis, for which the name S. barkulensis subsp. lavasanensis subsp. nov. is proposed. Culture extrac...
04
DOI 10.1021/acs.jnatprod.6c01039
Open DOI
Shape Shifting Proteusin Peptides and Their Multimodal Binding Interactions Underlie RiPP Biosynthesis
Ribosomally synthesized and post-translationally modified peptides (RiPPs) are produced through the selective recognition and enzymatic modification of precursor peptides. While canonical RiPP leader peptides are generally short and unst...
05
DOI 10.1021/acs.jnatprod.6c00877
Open DOI
Interaction Metabolomics to Discover Synergistic Constituents of Magnolia officinalis
Identifying combinations of molecules responsible for the biological activity of mixtures has long been a challenge for researchers in the natural products sciences. Recently, interaction metabolomics was described as a strategy for over...
06
DOI 10.1021/acs.jnatprod.6c00540
Open DOI
Marine Actin-Associated Agents Cause Distinct In Vivo Neuromuscular, Epithelia, and Organogenesis Phenotype Profiles in Caenorhabditis elegans
Natural products that target microfilaments are indispensable cell biology tools and have been explored as anticancer agents but are impeded by poor selectivity. Research utility and therapeutic potential would benefit from an expanded m...
07
DOI 10.1021/acs.jnatprod.6c00874
Open DOI
Computationally-Guided Structure Revision of the Chartellamides
Chartellamides A and B are heavily oxidized marine alkaloids that were isolated by Christophersen and co-workers from the marine bryozoan Chartella papyracea in 1987. The structures 1 and 2 were derived from MS and NMR-based structure el...
08
DOI 10.1021/acs.jnatprod.6c00830
Open DOI
Eudesmane Sesquiterpenoids from Dregea Volubilis Suppress Kidney Stones via Akt Signalling to Inhibit Oxalate Biosynthesis in Drosophila
Dregea volubilis has long been used in traditional medicine for the treatment of urolithiasis, yet its bioactive constituents and molecular mechanisms remain largely undefined. Here, molecular networking-guided UPLC-ESI-MS/MS analysis en...
09
DOI 10.1021/acs.jnatprod.6c00863
Open DOI
Identification and Spatial Distribution of Long-Chain Alkyl Sulfates from the Solitary Ascidian Ascidiella aspersa
Long-chain alkyl sulfate 1, three new derivatives 2−4, and (−)-loliolide-3-sulfate (7) were isolated from the solitary ascidian Ascidiella aspersa. The structures of compounds 1−4 were elucidated by NMR spectroscopy, HRESI-MS/MS, and che...
10
DOI 10.1021/acs.jnatprod.6c00532
Open DOI
Phenolic Metabolites as Therapeutics for Chronic Diseases: One Researcher’s PAINS Is Another’s Translatable Polypharmacology
Phenols, natural and semisynthetic compounds in which a hydroxylated or oxygenated aromatic scaffold is a defining structural feature, occupy a paradoxical position in drug discovery. On the one hand, these compounds are frequently scrut...
Bibliographical & Catalog Notes
Also issued online.
Articles mainly in English with some in French; summaries in English.
Published by the American Society of Pharmacognosy and the Lloyd Library and Museum.
Vol. 47, no. 2 (MAR-APR 1984)19890818 Notice published Printed on acid-free paper that meets the full ANSI standard for Permanent Paper